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Complex rearrangements of chromosome 15 in two patients with mild/atypical Prader Willi syndrome.
Salavoura, K; Kolialexi, A; Sofocleous, C; Kalaitzidaki, M; Pampanos, A; Kitsiou, S; Mavrou, A.
  • Salavoura K; Department of Medical Genetics, Athens University School of Medicine, Athens, Greece.
Genet Couns ; 19(2): 219-24, 2008.
Article en En | MEDLINE | ID: mdl-18618997
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Banco de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / Cromosomas Humanos Par 15 / Disomía Uniparental Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans / Infant / Male / Middle aged / Newborn Idioma: En Año: 2008 Tipo del documento: Article
Search on Google
Banco de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / Cromosomas Humanos Par 15 / Disomía Uniparental Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans / Infant / Male / Middle aged / Newborn Idioma: En Año: 2008 Tipo del documento: Article